Patent Grant
10344366
Disclosed is a coinage alloy for coinage comprising: nickel present in an amount from 13 wt. % to 16 wt. %, based on a total weight of the coinage alloy; zinc present in an amount from 25 wt. % to 32 wt. %, based on the total weight of the coinage alloy; manganese present in an amount from 1 wt. % to 4 wt. %, based on a total weight of the coinage alloy; copper; an electrical conductivity from 5% International Annealed Copper Standard (IACS) to 6% IACS measured in accordance with ASTM E1004-09 (2009); and a color comprising a yellowness vector b* that is from 5 to 10, m 5 to 10, based on CIE L*a*b* color space and determined in accordance with ASTM Standard E308-15 (2015).
Further disclosed is a process for making the coinage alloy, the process comprising: heating an alloying composition to a first temperature that is greater than or equal to an annealing temperature to form an annealing alloy, the alloying composition comprising: nickel present in an amount from 13 wt. % to 16 wt. %, based on a total weight of the alloying composition; zinc present in an amount from 25 wt. % to 32 wt. %, based on the total weight of the alloying composition; manganese present in an amount from 1 wt. % to 4 wt. %, based on a total weight of the alloying composition; and copper; and quenching, by cooling the annealing alloy from the first temperature to a second temperature that is less than the annealing temperature, under a condition effective to form the coinage alloy comprising the electrical conductivity and the yellowness vector b.
The following descriptions should not be considered limiting in any way. With reference to the accompanying drawings, like elements are numbered alike.
A detailed description of one or more embodiments is presented herein by way of exemplification and not limitation.
It has been discovered that a coinage alloy herein has unexpected and beneficial electrical, chemical, and physical properties suitable as a substitute for a cupronickel alloy for coins used in commerce, particularly coins in the United States that include the cupronickel alloy.
In an embodiment, the coinage alloy includes a plurality of transition metal elements, e.g., nickel, copper, zinc, manganese, or the like. The coinage alloy has a property effective for use of the coinage alloy in currency, e.g., as a coin. In a particular embodiment, the coinage alloy includes nickel, copper, manganese, and zinc in amount effective such that the coinage alloy has an electrical conductivity compatible with disposition in a coin that is compatible with a coin vending apparatus, a coin counter, or a coin identification machine.
In some embodiments, the coinage alloy has an electrical conductivity from 5% International Annealed Copper Standard (IACS) to 6% IACS measured in accordance with ASTM E1004-09 (2009). According to an embodiment, the coinage alloy has a disordered crystalline phase wherein atoms of the nickel, cooper, manganese, and zinc are randomly arranged in the disordered crystalline phase at room temperature in a post-annealed state. In some embodiments, a plurality of phases is present in the coinage alloy. In a certain embodiment, the plurality of phases includes face centered cubic, body centered cubic, or a combination thereof.
Materials used in a manufacture of the coinage alloy can contain a low level of an impurity such as a metal-, carbon-, or nitrogen-containing impurity. Such impurity can be present in the coinage alloy described herein, provided that the impurity is not present in an amount that significantly adversely affects the desired properties of the coinage alloy, in particular the electrical conductivity of the coinage alloy. Impurities can be present in the coinage alloy in a minor amount due to, e.g., leaching from contact with manufacturing equipment, uptake during processing of the coinage alloy, or components in an alloying composition that is used to make the coinage alloy.
The coinage alloy contains nickel in an amount from 13 weight percent (wt. %) to 16 wt. %, specifically 14.0 wt. % to 14.7 wt. %, based on a total weight of the coinage alloy. In an embodiment, the coinage alloy contains 14.4 wt. % nickel, based on a total weight of the coinage alloy.
The coinage alloy contains zinc in an amount from 25 wt. % to 32 wt. %, specifically 27.0 wt. % to 30.0 wt. %, based on a total weight of the coinage alloy. In an embodiment, the coinage alloy contains 28.2 wt. % zinc, based on a total weight of the coinage alloy.
The coinage alloy can contain manganese in an amount from 1 wt. % to 4 wt. %, specifically 2.0 wt. % to 2.4 wt. %, based on a total weight of the coinage alloy. In an embodiment, coinage alloy contains 2.2 wt. % manganese, based on a total weight of the coinage alloy.
The coinage alloy contains copper in an amount from 46 wt. % to 61 wt. %, specifically 52.9 wt. % to 57.0 wt. %, based on a total weight of the coinage alloy. In an embodiment, coinage alloy contains 55.2 wt. % copper, based on a total weight of the coinage alloy.
The coinage alloy can contain other elements such as Fe, Pb, P, or S, in an amount from 0 wt. % to 1.0 wt. %, specifically less than or equal to 0.5 wt. %, based on a total weight of the coinage alloy.
According to an embodiment, the coinage alloy contains nickel in an amount from 13 wt. % to 16 wt. %, zinc in an amount from 25 wt. % to 32 wt. %, manganese in an amount of 1 wt. % to 4 wt. %, based on the total weight of the coinage alloy, with the balance of the total weight being copper. That is, copper is present in an amount as a balance of the total weight of the coinage alloy.
According to an embodiment, the coinage alloy contains nickel in an amount from 13 wt. % to 16 wt. %, zinc in an amount from 25 wt. % to 32 wt. %, manganese in an amount of 1 wt. % to 4 wt. %, and copper in an amount from 46 wt. % to 61 wt. %, based on the total weight of the coinage alloy, with the balance of the total weight being copper. That is, copper is present in an amount as a balance of the total weight of the coinage alloy.
In a particular embodiment, the coinage alloy includes 14.4 wt. % Ni, 28.2 wt. %, Zn, 2.2 wt. % Mn, and Cu, based on a total weight of the coinage alloy.
In a particular embodiment, the coinage alloy includes 14.4 wt. % Ni, 28.2 wt. %, Zn, 2.2 wt. % Mn, and 55.2 wt. % Cu, based on the total weight of the coinage alloy.
According to an embodiment, the coinage alloy is referred to as C99R and includes Ni, Cu, Mn, and Zn that are present in an amount from 13 wt. % to 16 wt. % Ni, zinc in an amount from 25 wt. % to 32 wt. %, manganese in an amount of 1 wt. % to 4 wt. %, copper in an amount from 46 wt. % to 61 wt. %, and less than 0.2 wt. % of the impurity, based on a total weight of the coinage alloy, with the balance of the total weight being copper.
The coinage alloy can contain less than 1 weight percent (wt. %), less than 0.5 wt. %, or less than 0.1 wt. % of materials (e.g., the impurity) other than the nickel, copper, manganese, and zinc, based on the total weight of the coinage alloy, wherein a lower bound is 0 wt. % of the impurity.
An exemplary composition of the coinage alloy is shown in Table 1.
14-14.7
According to an embodiment, the coinage alloy can include a nominal composition of Cu-14.4Ni-28.2Zn-2.2Mn by mass.
In an embodiment, selected amounts of nickel, copper, manganese, and zinc are combined as an alloying composition at a temperature effective to produce a molten alloy of the alloying composition. A pure metal of the nickel, copper, zinc, and manganese can be combined as the alloying composition and then melted to form the molten alloy. The metal can be a powder, pellet, wire, shot, ingot, and the like; or in the form of scrap metal alloy where appropriate amounts of nickel, copper, zinc, and manganese are combined with the scrap alloy to produce the appropriate alloying composition.
According to an embodiment, a process for making the coinage alloy includes heating an alloying composition to a first temperature that is greater than or equal to an annealing temperature to form an annealing alloy, the alloying composition including: nickel present in an amount from 13 wt. % to 16 wt. %, based on a total weight of the alloying composition; zinc present in an amount from 25 wt. % to 32 wt. %, based on the total weight of the alloying composition; manganese present in an amount from 1 wt. % to 4 wt. %, based on a total weight of the alloying composition; and copper; and quenching, by cooling the annealing alloy from the first temperature to a second temperature that is less than the annealing temperature, under a condition effective to form the coinage alloy including the electrical conductivity and the yellowness vector b*.
In the process for making the coinage alloy, heating the alloying composition can include melting the alloying composition to form a molten alloy, and the process further can include cooling the molten alloy to form the annealing alloy. The annealing temperature can be from 600° C to 900° C, specifically from 700° C to 800° C, and more specifically from 725° C to 775° C. It is contemplated that the condition includes a cooling rate that is greater than or equal to air cooling from the first temperature to the second temperature. In some embodiments, the cooling rate is provided by water quenching the annealing alloy at a rate from 1° C per second (° C/s) to 1000° C, specifically from 10° C to 1000° C.
The process for making the coinage alloy further can include casting the molten alloy to form the annealing alloy in a solid state.
The process can further include subjecting the coinage alloy to thermo-mechanical processing to form an article such as a sheet, ingot, blank, coin, and the like. Exemplary, thermo-mechanical processing includes rolling, forging, cutting, stamping, pressing, and the like.
Melting the alloy composition occurs, e.g., at a temperature greater than or equal to a melting temperature of the nickel, copper, manganese, or zinc. Further, casting includes decreasing the temperature of the molten alloy below its melting point to form the annealing alloy. Casting can include cooling a container in which the molten alloy is disposed during melting the alloy composition. In some embodiments, casting includes disposing the molten alloy in a mold to form the annealing alloy and the coinage alloy at a temperature less than the melting point of the annealing alloy.
With the molten alloy formed from the alloying composition, the process includes cooling the molten alloy to a first temperature that is greater than or equal to an annealing temperature to form an annealing alloy; and quenching, by cooling the annealing alloy from the first temperature to a second temperature that is less than the annealing temperature, under a condition effective to form the coinage alloy.
In an embodiment, the annealing temperature is selected such that the annealing alloy is subjected to heat that is sufficient to produce a substantially disordered phase of the annealing alloy above the annealing temperature as the molten alloys solidifies to form the annealing alloy. In some embodiments, the molten alloy can be cooled below the annealing temperature and then reheated to a temperature greater than the annealing temperature to form the annealing alloy. Here, the annealing alloy is eventually transformed into the coinage alloy having the disordered crystalline phase as the annealing alloy is cooled below the annealing temperature. The annealing temperature can depend on the elemental composition of the annealing alloy (e.g., provided by the alloying composition) and can be from 600° C to 900° C, specifically from 700° C to 800° C, and more specifically from 725° C to 775° C. In an embodiment, the condition for quenching the temperature of the annealing composition to less than the annealing temperature includes a cooling rate that is greater than or equal to that cooling rate provided by air cooling from the first temperature to the second temperature. In a certain embodiment, the cooling rate is greater than or equal to the cooling rate of water quenching from the first temperature to the second temperature to form the coinage alloy from the annealing alloy. In some embodiments, the cooling rate is from 1° C/s to 1000° C/s, specifically from greater than or equal to 10° C/s. It is contemplated that the cooling rate can be from 104° C/s to 105° C/s for certain articles that include the coinage alloy.
In an embodiment, the coinage alloy has a face centered cubic phase. Here, the annealing temperature is selected such that the annealing alloy is subjected to heat that is sufficient to produce the face centered cubic phase in the annealing alloy above the annealing temperature as the molten alloys solidifies to form the annealing alloy. Thereafter, the annealing alloy is cooled below the annealing temperature at a rate to form the coinage alloy having the face centered cubic phase. The annealing temperature can depend on the elemental composition of the annealing alloy (e.g., provided by the alloying composition) and can be from 600° C to 900° C, specifically from 700° C to 800° C, and more specifically from 725° C to 775° C. In an embodiment, the condition for quenching the temperature of the annealing composition to less than the annealing temperature includes a cooling rate that is greater than or equal to that cooling rate provided by air cooling from the first temperature to the second temperature. In a certain embodiment, the cooling rate is greater than or equal to the cooling rate of water quenching from the first temperature to the second temperature to form the coinage alloy from the annealing alloy. In some embodiments, the cooling rate is from 1° C/s to 1000° C/s, specifically from greater than or equal to 10° C/s. It is contemplated that the cooling rate can be from 10° C/s to 105° C/s for certain articles that include the coinage alloy.
With reference to
At time t0, the alloying composition is at temperature T0. From time t0 to time t1, the alloying composition is heated from temperature T0 to melting temperature TM to melt the components of the alloying composition and to form the molten alloy. From time t2 to time t3, the molten alloy is cooled from melting temperature TM to first temperature T1 to form the annealing alloy in a solid state from a fluid state of the molten alloy. From time t4 to time t5, the temperature decreases from first temperature T1 (here, greater than annealing temperature TA) to second temperature T2 as the coinage alloy is formed from the annealing alloy.
In some embodiments, the annealing alloy and the coinage alloy have a same atomic ordering, e.g., first atomic ordering AO1. In certain embodiments, the coinage alloy and the annealing alloy have different atomic orderings, wherein the annealing alloy has first atomic ordering AO1, and the coinage alloy has second atomic ordering AO2. As used herein, “atomic ordering” refers to a location of atoms of copper, nickel, zinc, and manganese, wherein the atomic ordering of the atoms is disordered when the probability of finding an atom of specific type (Cu, Ni, Zn, or Mn) is approximately equal for all atomic positions (lattice sites) in the crystal structure, and the atomic ordering of the atoms is ordered when certain atomic positions are preferred by different atoms (e.g. atomic position A contains nearly all Cu atoms and few Ni, Zn, and Mn atoms; while atomic position B contains almost no Cu atoms and mostly Ni, Zn, and Mn atoms). It will be appreciated that crystallinity is a characteristic of the coinage alloy or annealing alloy that is different from the atomic ordering of the coinage alloy or annealing alloy. With regard to crystallinity, the coinage alloy can be crystalline, wherein the atoms are position in a repeating unit cell such that the crystallinity of the coinage alloy is face centered cubic, body centered cubic, complex body centered cubic (A12 or A13, Mn prototype), L12 (Cu3Au prototype), L10 (CuAu prototype), and the like. Moreover, under certain formation conditions, the coinage alloy can be amorphous or amorphous with crystalline domains.
In an embodiment, with reference to
It is contemplated that quenching includes subjecting the annealing alloy at the first temperature (which is greater than or equal to annealing temperature TA) to a fluid to cool the annealing alloy at a selected cooling rate from the first temperature to below annealing temperature TA to form the coinage alloy.
In an embodiment, the cooling rate is sufficiently rapid such that the coinage alloy is formed with the disordered crystalline phase having a selected atomic ordering. Here, the fluid can be a gas, liquid, or a combination thereof. Exemplary gases include air (including individual components of air (e.g., N2, O2, Ar, H2O, and the like)), noble gases, polyatomic gases (e.g., H2, CO2, and the like), and the like. Exemplary liquids include water, betaine, an oil, and the like. The heat capacity of the fluid can be high such that the fluid can receive a considerable amount of heat from the annealing alloy or coinage alloy during quenching and provide a high quenching rate. Similarly, a volume of the fluid used can be effective to provide a low temperature, heat sink effective to quench rapidly the annealing alloy or coinage alloy such that the coinage alloy attains the disordered crystalline phase. The fluid can be selected to provide a volume or heat capacity to provide an isothermal environment at a selected temperature (e.g., room temperature, or a temperature such as from −20° C to 100° C) to which the annealing alloy or coinage alloy is subjected so that the temperature of the annealing alloy can be decreased rapidly from the first temperature (greater than the annealing temperature) to the second temperature (less than the annealing temperature) to provide the coinage alloy prepared with the disordered crystalline phase, selected electrical conductivity, color, or combination thereof.
In an embodiment, the cooling rate is sufficiently slow such that the coinage alloy is formed with an ordered crystalline phase having a selected atomic ordering. Here, the fluid can be a gas, liquid, or a combination thereof. Exemplary gases include air (including individual components of air (e.g., N2, O2, Ar, H2O, and the like)), noble gases, polyatomic gases (e.g., H2, CO2, and the like), and the like. Exemplary liquids include water, betaine, an oil, and the like. The heat capacity of the fluid can be selectively tailored to be sufficiently low such that the fluid can receive heat from the annealing alloy or coinage alloy during quenching and provide a low quenching rate to provide for the ordered atomic ordering. Similarly, a volume of the fluid used can be effective to provide a moderate temperature heat sink to quench slowly the annealing alloy or coinage alloy such that the coinage alloy attains the ordered crystalline phase. The fluid can be selected to provide a volume or heat capacity to provide an isothermal environment at a selected temperature (e.g., room temperature, or a temperature such as from −20° C to 100° C) to which the annealing alloy or coinage alloy is subjected so that the temperature of the annealing alloy can be decreased slowly from the first temperature (greater than the annealing temperature) to the second temperature (less than the annealing temperature) to provide the coinage alloy prepared with the ordered crystalline phase, selected electrical conductivity, color, or combination thereof.
In an embodiment, the annealing alloy includes the same elemental composition as the coinage alloy. Without wishing to be bound by theory, due to forming the annealing alloy at the first temperature (which is greater or equal to the annealing temperature of the coinage alloy), the atoms in the annealing alloy are arranged in a disordered phase such as a face-centered cubic phase at the first temperature. Rapidly quenching the annealing alloy from the first temperature to the second temperature does not provide enough time for the atoms to rearrange into an ordered crystalline phase. As a result, the atoms maintain the disordered crystalline phase at the second temperature (and cooler temperatures thereof) in the coinage alloy.
In some embodiments, the atoms in the annealing alloy are arranged in a disordered phase such as a face-centered cubic phase at the first temperature. Slowly quenching the annealing alloy from the first temperature to the second temperature to form the coinage alloy provides enough time for the atoms to rearrange into an ordered crystalline phase. As a result, the atoms rearrange into the ordered crystalline phase at the second temperature (and cooler temperatures thereof) in the coinage alloy.
According to an embodiment, the annealing alloy has a different phase from the coinage alloy, and the annealing alloy has a first electrical conductivity that is different from the electrical conductivity of the coinage alloy. In an embodiment, the annealing alloy and the coinage alloy have substantially identical electrical conductivities. Moreover, the annealing alloy can have a same or different hardness or color as the hardness or color of the coinage alloy.
In an embodiment, the alloying composition is heated and melted to form the molten alloy. The molten alloy is a fluid that is subjected to cooling to solidify to form the annealing alloy. The annealing alloy is subjected to annealing at the first temperature (which is greater than annealing temperature TA of the annealing alloy). At the first temperature, the annealing alloy has a single phase that has a face-centered cubic (FCC) microstructure. In some embodiments, the first temperature is, e.g., greater than 450° C, and the annealing alloy can be maintained at or above annealing temperature TA for a selected time, e.g., from a few minutes to several hours. Processing the annealing alloy includes cooling the annealing alloy rapidly from the annealing temperature to approximately room temperature to form the coinage alloy in the selected phase. Cooling can occur by fast quenching (e.g., water quenching) or another method with a selected cooling rate to provide the coinage alloy in the selected disordered phase.
According to an embodiment, the alloying composition is heated and melted to form the molten alloy. The molten alloy is a fluid that is subjected to cooling to solidify to form the annealing alloy. The annealing alloy is subjected to annealing at the first temperature (which is greater than annealing temperature TA of the annealing alloy). At the first temperature, the annealing alloy has a phase that has a face centered cubic structure. In some embodiments, the first temperature is, e.g., 700° C, and the annealing alloy can be maintained at or above annealing temperature TA for a selected time, e.g., from a few minutes to several hours. Processing the annealing alloy includes cooling the annealing alloy at selected cooling rate from the annealing temperature to approximately room temperature to form the coinage alloy in the ordered phase. Cooling can occur by slowly quenching (e.g., air quenching) or another method with the selected cooling rate to provide the coinage alloy in the ordered phase.
Processing to form the coinage alloy from the annealing alloy can include cold rolling, warm rolling, air quenching, water quenching, and the like.
In certain embodiments, an electrical conductivity or mechanical property of the coinage alloy is selectively tailored or tuned by providing a rate of quenching the annealing alloy from annealing temperature TA to second temperature T2 to control a degree of atomic-level short-range ordering, e.g., from a high-temperature disordered FCC crystal phase in the annealing alloy to a selected atomic ordering of the coinage alloy obtained by the quenching process, wherein the atomic ordering can be disordered or ordered. It is contemplated that a faster cooling rate provides decreased ordering with the coinage alloy having a higher conductivity and lower hardness mechanical property compared with the annealing alloy. It is further contemplated that a slower cooling rate provides increased ordering on an atomic level and concomitant electrical conductivity (e.g., lower electrical conductivity) and mechanical property (e.g., higher hardness) of the coinage alloy.
In an embodiment, a process for forming the coinage alloy includes determining (e.g., making a predictive model) a composition of the coinage alloy based on electrical conductivity a of the coinage alloy, wherein data used in the model can be empirical or theoretical data. In an embodiment, the coinage alloy includes Cu—Mn—Ni—Zn, and
The process also includes determining (e.g., from the model) an electrical conductivity dependence on an amount of Ni, Zn, Cu, Mn, and the like, or a combination thereof.
The process can include constructing a model for selection of an elemental composition the metal elements (i.e., Cu, Ni, Zn, and Mn) in the alloying composition, annealing alloy, or coinage alloy. Here, a thermodynamic database was constructed for the Cu—Mn—Ni—Zn quaternary alloy system from thermodynamic data available in published literature (e.g., Miettinen, “Thermodynamic description of the Cu—Ni—Zn system above 600° C,” Calphad 27, 263 (2003); Miettinen, “Thermodynamic description of the Cu—Mn—Ni system at the Cu—Ni side,” Calphad 27, 147 (2003); and Miettinen, “Thermodynamic description of the Cu—Mn—Zn system in the copper-rich corner,” Calphad 28, 313 (2004), the content of each of which is incorporated herein by reference). The database provided determination of equilibrium phase diagrams by calculation and for determination of a composition range for undesirable phases that may form in an alloy.
The process can include including electrical conductivity in the model and included an amount of Mn present for making the coinage alloy. A plurality of coinage alloys was made and characterized to provide experimental data to calibrate the model. Table 2 lists exemplary alloys produced.
Alloys designated C99A through C99F were alloys used to calibrate the quaternary electrical conductivity model. Again,
Without wishing to be bound by theory, it is believed that about half of the wt. % of Mn produces a given electrical conductivity as compared with the wt. % of Ni in the coinage alloy such that as the amount of Ni is reduced, the coinage alloy obtain a more yellow color based on the b* yellow color vector. The b* vector in the La*b* color space was used as a metric for a degree of yellowness of the coinage alloy. A maximum b* value can be selected, e.g., to be 10, to be 7, or the like depending on the degree of yellow color desired for the coinage alloy. To incorporate color, e.g., the degree of yellow color, into the process for selecting an elemental composition of the metals in the coinage alloy, an empirical model for the color vector b* as a function of atomic composition of the metals in the coinage alloy was constructed from the data for b* collected using the experimental alloys produced, e.g. those listed in Table 2.
The model also can include cost as a factor to determine an atomic composition of the coinage alloy for a selected electrical conductivity of the coinage alloy. Here, a summation of costs for each of the four metals, i.e., Cu, Mn, Ni, and Zn, in the coinage alloy were weighted by the amount (i.e., wt. %) of each metal for a given atomic composition of the coinage alloy, e.g., as provided in formula 1 as follows:
cost=Σi=14(ci)(mi) (1),
wherein cost can have units of currency per mass (e.g., $/kg); i is an index of summation over each metal (i.e., Cu, Mn, Ni, and Zn); c is a cost per mass of the i-th metal, and m is a mass fraction of the i-th metal in the coinage alloy. In an embodiment, costs are $7.8/kg for Cu, $2.3/kg for Mn, $14.5/kg, for Ni, and $2.1/kg for Zn.
In an embodiment, the coinage alloy includes between 0 wt. % Ni to 11.5 wt. % Ni. According to an embodiment, the coinage alloy is C99E-2 (see Table 2) and included a small amount of BCC phase in its microstructure. In a certain embodiment, the electrical conductivity model was used to predict an electrical conductivity of alloy C99G and provided an expected electrical conductivity of about 5.4% IACS. Coinage alloy C99G included slightly more Ni than coinage alloy C99E, which stabilized a single-phase FCC microstructure in coinage alloy C99G. The conductivity of coinage alloy C99G was experimentally determined to be 5.30±0.02% IACS when made by annealing the annealing alloy that was water quenched to form coinage alloy C99G. Additionally, coinage alloy C99G had yellowness vector b* that was 9.45.
In an embodiment, the model included determining an atomic composition for the coinage alloy based on a desired color for the coinage alloy. The color can be parameterized by using yellowness vector b*, which was incorporated into the model. According to an embodiment, the atomic composition of the coinage alloy was determined for an electrical conductivity of 5.4% IACS and arbitrary value of color vector b*. The atomic composition output from the model was used to make various coinage alloys that were subjected to characterization. The coinage alloy included alloys listed in Table 2 as C99E, C99G, C99K, C99N, C99P, and C99Q. These coinage alloy are more yellow than C99R based on their b* values and provide financial cost savings over C71300. Table 3 lists certain coinage alloys and their properties along with potential cost savings over alloy C71300 that is used in coins.
In an embodiment, the coinage alloy is C99R, wherein the b* vector is 9.45±0.15 and includes from 10 wt. % Ni to 15 wt. % Ni. In a certain embodiment, C99R has a nominal composition of Cu-14Ni-28.5Zn-2.5Mn. An electrical conductivity of C99R can be, e.g., 5.37±0.01% IACS produced from an annealing alloy under the A-WQ processing of the annealing alloy. Here, the A-WQ processing includes annealing at a temperature of 750° C for 30 min and quenching into room temperature water. For C99R, without wishing to be bound by theory, it is believed that electrical conductivity of C99R is not sensitive to the quenching rate of the annealing alloy during formation of the coinage alloy. The electrical conductivity of C99R changes less than 0.05% IACS when the annealing alloy is subjected to cooling by water quenching (high cooling rate) and furnace cooling (slow cooling rate), wherein substantially no atomic ordering occurs, or atomic ordering occurs has little effect on electrical conductivity of C99R.
In an embodiment, once the atomic composition of C99R was selected, the electrical conductivity model was used to specify composition limits for each of the metals.
In an embodiment, a process for making the coinage alloy includes heating an alloying composition to a first temperature that is greater than or equal to an annealing temperature to form an annealing alloy, the alloying composition including; nickel present in an amount from 13 wt. % to 16 wt. %, based on a total weight of the alloying composition; zinc present in an amount from 25 wt. % to 32 wt. %, based on the total weight of the alloying composition; manganese present in an amount from 1 wt. % to 4 wt. %, based on a total weight of the alloying composition; and copper; and quenching, by cooling the annealing alloy from the first temperature to a second temperature that is less than the annealing temperature, under a condition effective to form the coinage alloy comprising the electrical conductivity and the yellowness vector b*. In the process, heating the alloying composition includes melting the alloying composition to form a molten alloy; and cooling the molten alloy to the first temperature to form the annealing alloy. The annealing temperature can be from 700° C to 800° C; and the condition includes a cooling rate that is greater than or equal to air cooling from the first temperature to the second temperature. The process for making the also can include casting the molten alloy to form the annealing alloy in a solid state. In some embodiments, the copper is present in an amount as a balance of the total weight of the coinage alloy, e.g., in an amount from 46 wt. % to 61 wt. %, based on the total weight of the coinage alloy. The coinage alloy can include a disordered crystalline phase, wherein atoms of the nickel, copper, zinc, and manganese are randomly arranged in the disordered crystalline phase at room temperature in a post-annealed state. Moreover, the disordered crystalline phase can include a single phase. Further, the single phase can be a face-centered cubic phase.
In the process, the electrical conductivity of the coinage alloy can be produced from quenching the annealing alloy from the annealing temperature at a cooling rate effective to produce the coinage alloy in a disordered crystalline phase. The cooling rate can be greater than or equal to air cooling from the annealing temperature to room temperature.
The coinage alloy can have a yield strength from 80 MPa to 180 MPa, a hardness of the coinage alloy is from 80 VHN to 250 VHN, or a combination thereof. The electrical conductivity of the coinage alloy can be selected via the process such that a coin including the coinage alloy is acceptable as currency in a vending machine that accepts the coin.
In an embodiment, a coin blank includes the coinage alloy, wherein an electrical conductivity of the coin blank is substantially equivalent to the electrical conductivity of UNS C71300 alloy. According to an embodiment, a process for making the coin blank includes punching coin blanks from a material sheet; annealing the blanks at a selected annealing temperature or a selected annealing time, quenching the blanks at the annealing temperature for a selected time in a fluid bath (e.g., a water bath); subjecting the blanks to remove oxide scale formed during annealing (e.g., by pickling the blanks); disposing an anti-tarnish coating on the blanks; upsetting the blank by deforming the blank edges to form a coin rim; and striking a plurality of the coins. The coins can be packaged (e.g., bagged) and shipped for distribution. In some embodiments, a plurality of coins is made from the coin blanks, and the coins have an electrical conductivity that is substantially identical to that of the coinage alloy. In an embodiment, the coins have an acceptance rate of 100% with coin vending machines, coin counters, coin detectors, and the like.
The coinage alloy has beneficial, advantageous, and unexpected properties. A color of the coinage alloy is silvery-white, wherein the color has: an a*value that from −10 to 10 and specifically less than 2.5; and a b*value that from −20 to 10 and specifically less than 10.0, measured in accordance with the Commission of Illumination L*a*b* color space (CIELAB) and ASTM E308-15. The electrical conductivity of the coinage alloy is from 5% IACS to 6% IACS, as determined by an eddy current conductivity meter operating at a frequency from 60 to 480 kHz in accordance with ASTM E1004-09 (2009). In an embodiment, the electrical conductivity of the coinage alloy is from 5.1% IACS to 5.7% IACS. In a certain embodiment, the electrical conductivity of the coinage alloy is within ±0.2% IACS of the electrical conductivity of USN C71300 alloy. According to an embodiment, the electrical conductivity of the coinage alloy is effective such that the coin includes the coinage alloy is accepted by coin-operated vending machines in the United States. In a particular embodiment, the electrical conductivity of the coinage alloy is within ±0.2% IACS for coins that are accepted by coin-operated vending machines in the United States.
The coinage alloy has a mechanical property such that the coinage alloy can be subjected to mechanical modification such as stamping, wherein a sheet of the coinage alloy is formed into an article such as a coin. The coinage alloy can have a yield strength from 120 megapascals (MPA) to 180 MPa. Beneficially, the coinage alloy excellent resistance to discoloration and corrosion-wear resistance equal to or better than alloy C71300 (alloy currently used in US coins).
The coinage alloy has an initial work hardening coefficient from 0.08 to 0.15, calculated from a tensile stress-strain curve over a strain range from 0.01 to 0.1, using Hollomon's equation for the power law relationship between stress and plastic strain. A corrosion rate of the coinage alloy is effective so that the coinage alloy is applicable in in a currency application, e.g., in a currency coin used in commerce. The coinage alloy has excellent wear resistance such that the coinage alloy has a long lifetime of years, e.g., decades. A density of the coinage alloy is similar to cupronickel such that a coin that includes the coinage alloy has a same mass as a coin that includes cupronickel.
In an embodiment, the coinage alloy beneficially has an electrical conductivity such that the coinage alloy is a replacement for the USN C71300 alloy used in U.S. coinage applications.
In an embodiment, the coinage alloy includes a single phase. In a certain embodiment, the single phase includes face-centered cubic (FCC) arrangement of atoms. Without wishing to be bound by theory, it is believed that when cooling the annealing alloy from the first temperature to the second temperature to form the coinage alloy, the annealing alloy has an FCC structure, and an ordering reaction does not occur upon cooling to the second temperature such that the FCC structure is the only phase present in the coinage alloy. In some embodiments, even though an ordered phase (referred to as L12 and L10 with respect to phases) in ternary Cu—Ni—Zn systems are known to exist, embodiments of the coinage alloy do not include the ordered L12 or L10 phase, wherein the coinage alloy has the FCC phase substantially so that the coinage alloy can replace the UNS 71300 alloy in US coins such as five-cent coin (i.e., 5¢, $0.05 US dollar (USD)).
In an embodiment, the rate at which the annealing alloy is cooled from the first temperature is selectively controlled to produce the coinage alloy having the single phase disordered crystalline phase and selected electrical conductivity and hardness. Without wishing to be bound by theory, it is believed that the ordering reaction from FCC to L12 or L10 phase occurs rapidly at a certain cooling rate, and the degree of atomic ordering varies from completely atomically disordered to fully atomically ordered such that the atomic ordering depends on the quenching rate from annealing temperature TA to approximately room temperature. Accordingly, in an embodiment, the cooling rate is selected to be high enough to form selectively the coinage alloy from the annealing alloy, wherein the coinage alloy includes the disordered crystalline phase in an absence of the L12 or L10 phase.
The hardness of the coinage alloy is effective such that the coinage alloy can be subjected to mechanical deformation to produce an article such as a coin. The hardness can be a Vickers micro hardness from 80 HV02 (HV02 indicates the Vickers hardness number measured with a force of 0.2 kg) to 100 HV02, specifically less than 108 HV02. Mechanical deformation can include bending, stretching, cutting, and the like. In an embodiment, a sheet of the coinage alloy is formed and subjected to stamping to form an article such a plurality of coins.
The coinage alloy advantageously provides for seamless substitution of current cupronickel alloys used in certain currency, e.g., coins such as U.S. coins. In a particular embodiment, the coinage alloy is a replacement for cupronickel alloy (e.g., USN C71300 alloy) used in production by the United States Mint of five-cent U.S. coins (“nickels”).
It has been found that the coinage alloy can be used in currency applications due to its physical, chemical, or mechanical property. The coinage alloy can be cast or prepared into a selected format by, e.g., a process that includes thermo-mechanically processing (e.g., rolling, forging, and the like).
The coinage alloy is a seamless substitution for cupronickel in U.S. coin-making at a cost that is, e.g., 20% less than current cupronickel alloy processing. The electrical conductivity of the coinage alloy is substantially identical to the electrical conductivity of cupronickel alloy such that the coinage alloy is used as a coin with coin-operated vending machines, coin counters, coin identification machines, and the like.
Advantageously and unexpectedly, the conductivity of the coinage alloy is selected such that a coin including the coinage alloy is acceptable as currency in a vending machine that accepts the coin. Acceptance of the coin contemplates that an electrical signature (e.g., electrical conductivity) of the coin is equivalent to an electrical signature of currently available coins made with their current material when measured using current coin-sorting technology.
In an embodiment, the coinage alloy is used in a variety of applications that use a conductive metal having the electrical conductivity of the coinage alloy, e.g., as an electrical contact for an electronic device. An electrical contact formed using the coinage alloy can be used such that a first component and a second component are arranged in a spaced apart relation. The coinage alloy (or a composition comprising the coinage alloy) is disposed between and in physical contact with the first component and the second component to form an electrical path between the first component and the second component. The coinage alloy can be in a wide variety of forms to contact the first and the second component. The form may be, for example, a wire, cable, button, coating, and the like.
In an embodiment, the coinage alloy is a portion of a conductive contact in a connector, switch, or insert. Examples of the connector are a blade connector, push-on connector, crimp connector, multi-pin connector (e.g., a D-sub connector), bolt connector, set screw connector, lug, wedge connector, bolted connector, compression connector, coaxial connector, wall connector, surface mount technology (SMT) board connector, IPC connector, DIN connector, phone connector, plastic leaded chip carrier (PLCC) socket or surface mount connector, integrated circuit (IC) connector, ball grid array (BGA) connector, staggered pin grid array (SPA) connector, busbar connector, or the like. Switches include, e.g., a circuit breaker, mercury switch, wafer switch, dual-inline package (DIP) switch, reed switch, wall switch, toggle switch, in-line switch, toggle switch, rocker switch, microswitch, rotary switch, and the like. An insert can be, e.g., a transition washer, disc, tab, and the like.
The coinage alloy has a number of advantages. The coinage alloy has sufficient electrical conductivity to prevent development of an unacceptably high contact resistance. Use of the coinage alloy decreases use of precious metal plating of electrical contacts while conserving operational characteristics of such current-carrying contacts. In addition, the coinage alloy is manufactured from widely available materials.
The articles and processes herein are illustrated further by the following Examples, which are non-limiting.
A Cu-14.4Ni-28.2Zn-2.2Mn coinage alloy was made by melting together the appropriate amounts of the pure elements Cu, Ni, Zn, and Mn required to produce a 1 kg ingot of the coinage alloy composition and pour casting into a copper mold; hot rolling the ingot into a sheet 0.065 inches in thickness; annealing in air at 750° C for 30 min; quenching into room temperature water.
The Cu-14.4Ni-28.2Zn-2.2Mn coinage alloy exhibited the properties: electrical conductivity of 5.37% IACS; color vector of L=84.31, a*=−0.40, and b*=7.44; Vickers microhardness of 93 VHN; tensile yield strength of 118 MPa; ultimate tensile strength of 273 MPa; strain to failure of 0.55; initial work hardening coefficient of 0.11.
A Cu-7.5Ni-30.9Zn-4.6Mn coinage alloy was made by melting together the appropriate amounts of the pure elements Cu, Ni, Zn, and Mn required to produce a 200 g ingot of the coinage alloy composition and pour casting into a copper mold; hot rolling the ingot into a sheet 0.065 inches in thickness; annealing in air at 750° C for 30 min; quenching into room temperature water.
The Cu-7.5Ni-30.9Zn-4.6Mn coinage alloy exhibited properties including: electrical conductivity of 5.30% IACS; color vector of L=84.71, a*=−0.32, and b*=9.45; Vickers microhardness of 90 VHN.
While one or more embodiments have been shown and described, modifications and substitutions may be made thereto without departing from the spirit and scope of the invention. Accordingly, it is to be understood that the present invention has been described by way of illustrations and not limitation. Embodiments herein can be used independently or can be combined.
Reference throughout this specification to “one embodiment,” “particular embodiment,” “certain embodiment,” “an embodiment,” or the like means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment. Thus, appearances of these phrases (e.g., “in one embodiment” or “in an embodiment”) throughout this specification are not necessarily all referring to the same embodiment, but may. Furthermore, particular features, structures, or characteristics may be combined in any suitable manner, as would be apparent to one of ordinary skill in the art from this disclosure, in one or more embodiments.
All ranges disclosed herein are inclusive of the endpoints, and the endpoints are independently combinable with each other. The ranges are continuous and thus contain every value and subset thereof in the range. Unless otherwise stated or contextually inapplicable, all percentages, when expressing a quantity, are weight percentages. The suffix “(s)” as used herein is intended to include both the singular and the plural of the term that it modifies, thereby including at least one of that term (e.g., the colorant(s) includes at least one colorants). “Optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where the event occurs and instances where it does not. As used herein, “combination” is inclusive of blends, mixtures, alloys, reaction products, and the like.
As used herein, “a combination thereof” refers to a combination comprising at least one of the named constituents, components, compounds, or elements, optionally together with one or more of the same class of constituents, components, compounds, or elements.
All references are incorporated herein by reference.
The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. “Or” means “and/or.” Further, the conjunction “or” is used to link objects of a list or alternatives and is not disjunctive; rather the elements can be used separately or can be combined together under appropriate circumstances. It should further be noted that the terms “first,” “second,” “primary,” “secondary,” and the like herein do not denote any order, quantity, or importance, but rather are used to distinguish one element from another. The modifier “about” used in connection with a quantity is inclusive of the stated value and has the meaning dictated by the context (e.g., it includes the degree of error associated with measurement of the particular quantity).
This invention was made with United States Government support from the National Institute of Standards and Technology. The Government has certain rights in the invention.
| Number | Name | Date | Kind |
|---|---|---|---|
| 2101087 | Munson | Dec 1937 | A |
| 2445868 | Berwick | Jul 1948 | A |
| 3234014 | McLain | Feb 1966 | A |
| 3640781 | Ansuini | Feb 1972 | A |
| 4003715 | Cascone | Jan 1977 | A |
| 4147568 | Marechal | Apr 1979 | A |
| 5885376 | Suzuki | Mar 1999 | A |
| 5997663 | Kita et al. | Dec 1999 | A |
| 6340446 | Kita et al. | Jan 2002 | B1 |
| 6432556 | Brauer | Aug 2002 | B1 |
| 9951406 | Lass | Apr 2018 | B2 |
| 20100061884 | Clark et al. | Mar 2010 | A1 |
| 20130189540 | McDaniel et al. | Jul 2013 | A1 |
| 20140112822 | Tanaka et al. | Apr 2014 | A1 |
| 20160068940 | Lass | Mar 2016 | A1 |
| 20180105912 | Lass | Apr 2018 | A1 |
| 20180105913 | Lass | Apr 2018 | A1 |
| Number | Date | Country |
|---|---|---|
| 19802246 | Jul 1999 | DE |
| 2287954 | Oct 1995 | GB |
| Entry |
|---|
| English translation of DE 19802246, Jul. 1999; 6 pages. |
| Number | Date | Country | |
|---|---|---|---|
| 20180105911 A1 | Apr 2018 | US |
